US Drug Recall Register
Class I · High risk Terminated Initiated Oct 23, 2023 (3 years ago)

Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Failed Content Uniformity Specifications

What was recalled

Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups (NDC 0904-7079-24), 50 per case (NDC 0904-7079-57), Rx only, Major Pharmaceuticals Livonia, MI 48152

Recalling firm
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
NDC code
0904-7079-24
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0153-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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